Taxachitriene A

95%

Reagent Code: #241448
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CAS Number 167906-74-3

science Other reagents with same CAS 167906-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 636.684 g/mol
Formula C₃₂H₄₄O₁₃
thermostat Physical Properties
Boiling Point 678.1±55.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.2±0.1g/ml
Storage 2-8℃

description Product Description

Used in advanced organic synthesis as a key intermediate for the development of bioactive natural product derivatives. Shows potential in pharmaceutical research due to its unique tricyclic framework, which exhibits anti-inflammatory and cytotoxic activities in preliminary biological assays. Employed in structure-activity relationship (SAR) studies to design new therapeutic agents targeting cancer cell lines. Its complex ring system also serves as a model compound for testing novel synthetic methodologies, particularly in stereoselective cyclization reactions.

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inventory 5mg
10-20 days ฿34,270.00

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Taxachitriene A
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Used in advanced organic synthesis as a key intermediate for the development of bioactive natural product derivatives. Shows potential in pharmaceutical research due to its unique tricyclic framework, which exhibits anti-inflammatory and cytotoxic activities in preliminary biological assays. Employed in structure-activity relationship (SAR) studies to design new therapeutic agents targeting cancer cell lines. Its complex ring system also serves as a model compound for testing novel synthetic methodologies,
Used in advanced organic synthesis as a key intermediate for the development of bioactive natural product derivatives. Shows potential in pharmaceutical research due to its unique tricyclic framework, which exhibits anti-inflammatory and cytotoxic activities in preliminary biological assays. Employed in structure-activity relationship (SAR) studies to design new therapeutic agents targeting cancer cell lines. Its complex ring system also serves as a model compound for testing novel synthetic methodologies, particularly in stereoselective cyclization reactions.
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